A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16295206



Internal ID20504424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92400101..92409596hg38UCSC Ensembl
chr10:94159858..94169353hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg389496
hg199496
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4748754
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16295206
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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